Filie JD - Search Results

1

Mouse gastric mucin: cloning and chromosomal localization.

Shekels LL, Lyftogt C, Kieliszewski M, Filie JD, Kozak CA, Ho SB. Shekels LL, et al. Among authors: filie jd. Biochem J. 1995 Nov 1;311 ( Pt 3)(Pt 3):775-85. doi: 10.1042/bj3110775. Biochem J. 1995. PMID: 7487932 Free PMC article.

2

Molecular cloning, characterization, and genetic mapping of the cDNA coding for a novel secretory protein of mouse. Demonstration of alternative splicing in skin and cartilage.

Bhalerao J, Tylzanowski P, Filie JD, Kozak CA, Merregaert J. Bhalerao J, et al. Among authors: filie jd. J Biol Chem. 1995 Jul 7;270(27):16385-94. doi: 10.1074/jbc.270.27.16385. J Biol Chem. 1995. PMID: 7608209 Free article.

3

Genetic mapping of the alpha 1 and alpha 2 (IV) collagen genes to mouse chromosome 8.

Filie JD, Burbelo PD, Kozak CA. Filie JD, et al. Mamm Genome. 1995 Jul;6(7):487. doi: 10.1007/BF00360662. Mamm Genome. 1995. PMID: 7579895 No abstract available.

4

Genetic mapping of the mouse ferritin light chain gene and 11 pseudogenes on 11 mouse chromosomes.

Filie JD, Buckler CE, Kozak CA. Filie JD, et al. Mamm Genome. 1998 Feb;9(2):111-3. doi: 10.1007/s003359900699. Mamm Genome. 1998. PMID: 9457670

5

Differential expansion of the N-formylpeptide receptor gene cluster in human and mouse.

Gao JL, Chen H, Filie JD, Kozak CA, Murphy PM. Gao JL, et al. Among authors: filie jd. Genomics. 1998 Jul 15;51(2):270-6. doi: 10.1006/geno.1998.5376. Genomics. 1998. PMID: 9722950

6

Rat phenol-preferring sulfotransferase genes (Stp and Stp2): localization to mouse chromosomes 7 and 17.

Khan AS, Taylor BR, Filie JD, Ringer DP, Kozak CA. Khan AS, et al. Among authors: filie jd. Genomics. 1995 Mar 20;26(2):417-9. doi: 10.1016/0888-7543(95)80233-c. Genomics. 1995. PMID: 7601475

7

Murine chromosomal location of the mu and kappa opioid receptor genes.

Kozak CA, Filie J, Adamson MC, Chen Y, Yu L. Kozak CA, et al. Genomics. 1994 Jun;21(3):659-61. doi: 10.1006/geno.1994.1331. Genomics. 1994. PMID: 7959748

8

A de novo G+1-->A mutation at the alpha 2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI type IV proband.

Filie JD, Orrison BM, Wang Q, Lewis MB, Marini JC. Filie JD, et al. Hum Mutat. 1993;2(5):380-8. doi: 10.1002/humu.1380020510. Hum Mutat. 1993. PMID: 8257992

9

Intractable vasculitis, resorptive osteolysis, and immunity to type I collagen in type VIII Ehlers-Danlos syndrome.

Hoffman GS, Filie JD, Schumacher HR Jr, Ortiz-Bravo E, Tsokos MG, Marini JC, Kerr GS, Ling QH, Trentham DE. Hoffman GS, et al. Among authors: filie jd. Arthritis Rheum. 1991 Nov;34(11):1466-75. doi: 10.1002/art.1780341119. Arthritis Rheum. 1991. PMID: 1953824 Review.

10

A patient with Ehlers-Danlos syndrome type VI is homozygous for a premature termination codon in exon 14 of the lysyl hydroxylase 1 gene.

Walker LC, Marini JC, Grange DK, Filie J, Yeowell HN. Walker LC, et al. Mol Genet Metab. 1999 May;67(1):74-82. doi: 10.1006/mgme.1999.2824. Mol Genet Metab. 1999. PMID: 10329027

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

11 results

Search Page

Filters